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Cognitive function after liver transplantation comparing Tacrolimus formulations
EU CTIS ID: 2024-513963-22-00
What this study is testing
To determine whether once-daily formulation of Tacrolimus (Envarsus ®) improves subjective impression of attention and memory performance compared to twice-daily formulation of Tacrolimus
- Therapeutic use (Phase IV)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- Written informed consent
- Age 20 to 75 years
- After 12 months post liver transplantation
- Immunosuppression with a twice daily formulation of Tacrolimus
- Application of the same active Tacrolimus twice daily formulation ≥3 months
- At least mild cognitive impairment
You likely can't join if
- Dialysis treatment during the previous 30 days
- Deafness and/or blindness
- Pregnancy/breastfeeding mothers
- Current participation in another study
- Every other aspect that, in the eye of investigator, makes the patient unable to comply with study procedures
The study team makes the final eligibility decision.
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.